Report – Analysis of FDA 483s Issued to Excipient Manufacturers Since 2000
By
Jerry Chapman
,
This report looks across all excipient manufacturer 483s, including the one to DuPont that Redica Systems has in our Platform, and reviews the recurring concerns found by FDA in the last 20+ years.
Other areas examined in the report are:
An in-depth view of why DuPont Nutrition was inspected
Implications of the warning letter
483 Observation Analysis using Redica Systems data
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If you have trouble with the form, please contact events@redica.com.